Chr Mutation (hg38) CAid Gene Transcript Linkouts
6g.157181168G>TCA366228517ARID1Bc.3545G>T (p.Gly1182Val)
c.3614G>T (p.Gly1205Val)
c.3833G>T (p.Gly1278Val)
c.1718G>T (p.Gly573Val)
c.3584G>T (p.Gly1195Val)
c.3296G>T (p.Gly1099Val)
c.1862G>T (p.Gly621Val)
c.1025G>T (p.Gly342Val)
c.659G>T (p.Gly220Val)
c.3704G>T (p.Gly1235Val)
n.1701G>T
c.1072G>T
c.986G>T
n.370G>T
c.1046G>T (p.Gly349Val)
c.1205G>T (p.Gly402Val)
c.3335G>T (p.Gly1112Val)
c.1721G>T (p.Gly574Val)
c.497G>T (p.Gly166Val)
c.906G>T
c.3455G>T (p.Gly1152Val)
c.2534G>T (p.Gly845Val)
c.2354G>T (p.Gly785Val)
c.2114G>T (p.Gly705Val)
c.1733G>T (p.Gly578Val)
c.596G>T (p.Gly199Val)
c.3665G>T (p.Gly1222Val)
c.3566G>T (p.Gly1189Val)
c.3536G>T (p.Gly1179Val)
c.3506G>T (p.Gly1169Val)
c.3377G>T (p.Gly1126Val)
c.3356G>T (p.Gly1119Val)
n.3748G>T
dbSNP
6g.157181168G>CCA366228512ARID1Bc.3545G>C (p.Gly1182Ala)
c.3614G>C (p.Gly1205Ala)
c.3833G>C (p.Gly1278Ala)
c.1718G>C (p.Gly573Ala)
c.3584G>C (p.Gly1195Ala)
c.3296G>C (p.Gly1099Ala)
c.1862G>C (p.Gly621Ala)
c.1025G>C (p.Gly342Ala)
c.659G>C (p.Gly220Ala)
c.3704G>C (p.Gly1235Ala)
n.1701G>C
c.1072G>C
c.986G>C
n.370G>C
c.1046G>C (p.Gly349Ala)
c.1205G>C (p.Gly402Ala)
c.3335G>C (p.Gly1112Ala)
c.1721G>C (p.Gly574Ala)
c.497G>C (p.Gly166Ala)
c.906G>C
c.3455G>C (p.Gly1152Ala)
c.2534G>C (p.Gly845Ala)
c.2354G>C (p.Gly785Ala)
c.2114G>C (p.Gly705Ala)
c.1733G>C (p.Gly578Ala)
c.596G>C (p.Gly199Ala)
c.3665G>C (p.Gly1222Ala)
c.3566G>C (p.Gly1189Ala)
c.3536G>C (p.Gly1179Ala)
c.3506G>C (p.Gly1169Ala)
c.3377G>C (p.Gly1126Ala)
c.3356G>C (p.Gly1119Ala)
n.3748G>C
dbSNP
6g.157181168G>ACA248922ARID1Bc.3545G>A (p.Gly1182Asp)
c.3614G>A (p.Gly1205Asp)
c.3833G>A (p.Gly1278Asp)
c.1718G>A (p.Gly573Asp)
c.3584G>A (p.Gly1195Asp)
c.3296G>A (p.Gly1099Asp)
c.1862G>A (p.Gly621Asp)
c.1025G>A (p.Gly342Asp)
c.659G>A (p.Gly220Asp)
c.3704G>A (p.Gly1235Asp)
n.1701G>A
c.1072G>A
c.986G>A
n.370G>A
c.1046G>A (p.Gly349Asp)
c.1205G>A (p.Gly402Asp)
c.3335G>A (p.Gly1112Asp)
c.1721G>A (p.Gly574Asp)
c.497G>A (p.Gly166Asp)
c.906G>A
c.3455G>A (p.Gly1152Asp)
c.2534G>A (p.Gly845Asp)
c.2354G>A (p.Gly785Asp)
c.2114G>A (p.Gly705Asp)
c.1733G>A (p.Gly578Asp)
c.596G>A (p.Gly199Asp)
c.3665G>A (p.Gly1222Asp)
c.3566G>A (p.Gly1189Asp)
c.3536G>A (p.Gly1179Asp)
c.3506G>A (p.Gly1169Asp)
c.3377G>A (p.Gly1126Asp)
c.3356G>A (p.Gly1119Asp)
n.3748G>A
ClinVar dbSNP COSMIC COSMIC

Number of alleles fetched